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Thursday, January 29th, 2026

Climbing Fast

Monday, January 5th, 2026: Chiricahuas, Hikes, Silver, Southeast Arizona.

After last Sunday’s breakthrough – hiking to a peak with a spectacular view, after months of frustrating “recovery” hikes – I was hoping for more of the same. But most spectacular hikes on my list either involve too much distance and elevation, or too much bushwhacking. I finally decided to drive over to Arizona yet again, for a peak hike that, when I’m in top condition, would only take a half day. At this stage in my recovery it would advance me a notch, to nearly ten miles out-and-back and over 3,000 accumulated vertical feet.

The day was forecast to be cloudy but with mild temps. However, for the third day in a row – after getting both flu and COVID shots four days ago – I woke up with a migraine and a body that ached from head to feet. Side effects are not supposed to last that long, but it was Sunday and I was not going to miss my hike.

This is the most popular trail in the most popular part of the range, so despite the winter season and gloomy skies, I wasn’t surprised to find three vehicles at the trailhead. A quarter of a mile up I passed a retired-looking couple returning – most people are only in shape for the first mile or so.

I was making good time – clearly recovering my cardio capacity. I’d hoped endorphins would reduce my pain, but by the time I’d gone about 3/4 of a mile I knew I would need pain meds. I’d gotten a late start, and it was also time for a snack. And stopping to dig in my pack, I discovered that I’d failed to bring any food.

This has never happened before! I use a list to pack for a hike. Everything I need is at hand, in its regular place. But I’ve gotten in the bad habit of packing first and checking my list afterwards. And at home this morning, with the splitting headache making me dizzy and confused, I’d just glanced at the food part and assumed it was already packed.

A foundation of my healthy lifestyle is to eat for activity, in a weekly cycle timed with my hikes and workouts. I avoid eating more than I’ll need, but before, during, and after strenuous activity, I always eat and drink what my body needs to recover and build muscle, but no more. There on the mountainside, my whole body hurting, I knew if I turned back to get food at the country store, I wouldn’t be able to complete the hike. I also knew I must be carrying a little fat, somewhere, that my body could turn into energy to finish this damn hike.

So in the title above, “climbing” is an adjective, and “fast” is a noun.

As soon as I resumed hiking in this familiar high desert habitat, I began seeing it in the way I’d been trained long ago – as a natural cupboard, potentially full of provisions. What was here that I could eat? It’s January, one of the worst months for plant food. There would be lots of pinyon pine up above, but the cones would’ve opened months ago, any remaining nuts shriveled and dried. I found one trapped inside a cone but almost cracked a tooth on it, it was so hard.

I immediately thought of cactus fruit. There were lots of prickly pear, but the only remaining fruit were all shriveled up. I’d never heard of anyone eating the yellow fruit of the cane cholla, and there were few here, but I finally came upon one and checked it out. Most of the remaining fruit were unripe, but looking closely at a few yellow ones, it appeared there were no glochids, so I pulled them off and cut them open.

Glochids are tiny, almost invisible hairlike spines that surround the areoles of cacti, where the hard spines emerge. The fruit can be free of spines, but the dozens of tiny glochids will still work their way into your skin and torment you for days, so cactus fruit are normally handled with some kind of tool. My desperation, and the darkness of the day, lulled me into complacency.

After cutting the fruit in half and scraping out the rock-hard seeds, I turned the fruit inside out and scraped at the pulp with my teeth. Even in the greener fruit it was sweet, but there was precious little of it.

I dumped the rest in my shirt pocket and resumed hiking. And now my fingers began burning – glochids after all!

The first 2-1/2 miles climbs 1,200 vertical feet to a shoulder on the north slope, where the trail turns back almost due south into a deep cove. At the top, colorful cliffs and rock formations span both sides of a steep drainage forested with ponderosa pines and Douglas-firs. The trail switchbacks and traverses toward and through the rocks, then out onto the opposite slope. The complicated stretch through those rocks is the most interesting part of the hike.

Emerging onto the opposite slope on a steep stretch of trail, I spotted a leashed dog ahead, and looked for a place to step off and let the owner by. It was a twenty-something couple – they both smiled and thanked me. Past there, it’s a long traverse across a steep slope with dramatic rock formations looming above, eventually entering a patch of fir forest that was particularly dark today.

Approaching the west side of the peak, the trail finally switches back eastward behind huge ramparts of stone, where ten switchbacks of nearly equal length lead you up past the rocks toward the crest. After the long slog on the switchbacks it’s always a surprise to find yourself facing only a short, easy walk to the saddle.

The true peak is a short distance east, but the old fire lookout has the view – if you can handle the precarious, vertiginous concrete steps. The lookout itself burned decades ago – all that’s left now is the concrete foundation.

I’ve been up here in all seasons – there would normally be snow now – and never tire of it.

The only thing I’d brought with any nutritional value was a packet of electrolyte supplement, containing sugar. I’d consumed that hours ago, but didn’t feel hungry. But I did expect my body to start complaining on the way down. As per last week, I dug out the trekking poles to make it easier on my injured knee. And I finally figured out how to use them – which is basically not to push down on them at all, just dangle and tap – until you reach a rocky or steep point where they can help with balance.

Generating less heat on the way down, I pulled my sweater on, and the extra pressure drove the glochids on the fruit in my pocket into my chest, so I transferred them to my pack, and eventually tossed them away. But by then, the damage was done, and I wouldn’t be able to remove them from my chest until I got home.

Much worse, the chronic inflammation in the ball of my left foot had been triggered in the past week – by a new exercise the physical therapist had given me – and this more challenging hike was bringing it out. So I had three thousand feet to descend with two bad legs, slowing me down and forcing me to rely more on the poles, which in turn put more strain on my injured shoulder. I’d had to take more pain pills in the past three days than ever before.

This also highlights another failure of our healthcare system – a hard one to understand, an impossible one to solve. Individualist and competitive social behavior lead to a capitalist economy and the nation-state, imperialism produces reductive science, and the result is healthcare institutions that compete against each other and specialist practitioners that are ignorant outside their fields. So with multiple injuries and health conditions, I’m treated at many different facilities by many different providers, none of whom have access to all my information, and none of whom have time, when they see me, to figure out whether their treatments will have negative consequences.

In the end, the only thing I can always depend on is pain pills – opioids, the “evil” that misguided, Puritanical crusaders keep making it harder and harder for us to get. So I ended my hike a starving wreck, with the pain mercifully shifted into the background for a few hours.

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Winter Wonderland

Monday, January 26th, 2026: Hikes, Holt, Mogollon Mountains, Southwest New Mexico.

I’d spent September through November rebuilding my hiking capacity. By December I felt like I was on a path to recovery, but life spun out of my control. I went from 8-9 hikes per month, to only 5 hikes in the past two months.

Still, my brain was stuck in recovery mode, so even with 2-3 weeks of down time between them, every hike had to be more challenging than the last, leaving me in lots of unnecessary pain. Before this latest hike, I even wrote a big note to myself: Take it Easy! But we’d had a two-day storm, and in the end, the only hike that appealed to me was one that would get me up into some snow. It was an old favorite hike I’ve done many times, and this would be the first time since my knee injury that I would try to reach the first milestone – a spring just below the 9,500 foot crest.

Under clear skies, the air temperature in the shade was in the 20s as I began the traverse into the canyon. In a sunny spot where the dirt of the trail had melted, I came upon the bootprints of a lone hiker – probably a man – who had gone out and back yesterday.

Expecting snow, I was wearing my winter boots for the first time in almost two years, and after entering the wilderness area in the first half mile, the stiff boots had triggered a pressure point on the inside of my right ankle, and it felt like someone was driving a nail into the joint.

Three options: (1) dose myself with pain meds, which I hate to do this early in the day, (2) stop, take off my boot, roll back my socks and thermal bottoms, dig the adhesive-backed felt out of my backpack and cut a piece to fit around the hurt area, or (3) keep going and hope it would get better. (Actually, a 4th option would be alternate lacing, but I’m not thinking too well these days.)

I chose option 3, and instead of it getting better, I just decided to put up with it, every step hurting equally for the next 4-1/2 miles.

It’s about a mile to the canyon bottom. From there, the trail up the creek bank is easy for another mile, but after that, the grade up the canyon increases steadily for another mile, to the base of switchbacks that climb to the crest.

And I discovered that, probably because I’d had so many inactive intervals between hikes recently, I’d lost much of my cardio conditioning. Any grade at all – even less than 5 percent – immediately left me out of breath. The farthest I could go without stopping was about 100 feet. How could I possibly make it up those increasingly steep switchbacks?

One thing that kept me motivated was the gaps in the forest opened up by drought-induced tree mortality, providing better views of the rock formations on the slopes above. And at one point I got a glimpse of snow-laden trees on the crest. They were two thousand feet above me – at this rate, and in this much pain, how would I ever make it?

I couldn’t remember ever having to stop so often, but every time, after long minutes of regaining my breath, I continued for another 50-100 feet. I expected deeper snow in shady spots ahead, and my pant legs were already getting soaked from creek crossings, so in the first bare spot I pulled out and strapped on my gaiters.

In shady spots where the snow was deepest, I found the other hiker’s deep tracks overlaid with an inch or so of overnight snow. I knew if I could make it past the lower steep part of the switchbacks, I would have a much easier time on the long stretches traversing the upper slopes of this side canyon. Holding that thought, I finally reached the overlook, on an outlying shoulder at 8,400 feet. This is always an inspiring moment, because you actually look down on the mountain that was looming above you while you were ascending the canyon bottom.

I’d made it most of the way to the crest – but the steepest climb was still ahead of me. As before, I just doggedly continued in very short stages. The steep part faces west and was mostly snow-free. And I eventually made it, to the higher shoulder with a little rock outcrop which is where I stopped the first time I hiked this trail, seven years ago.

Past that outcrop, the trail turns back into shade and gets steeper – hence it held snow, mostly about 4 inches deep. I hadn’t planned to go any farther. But the sight of untracked snow ahead – the other hiker had stopped either at the overlook below, or here at the little outcrop – tantalized me. I believed I had plenty of time, and it’s only another quarter mile to the spring.

What I’d forgotten is that this stretch of the trail crosses two deep gullies on a steep, shady slope where snow drifts two or three times as deep. The first drift completely obliterated the trail. If I lost my balance or slipped crossing that drift, I would slide 60 feet down a 45 degree slope before hitting a log.

But I’d brought trekking poles, and I figured I would just cross the drift a step at a time, taking short steps and kicking a foothold in the drift before the next step. With that, and the poles for balance, it took me about fifteen minutes to traverse 50 feet – but it worked.

Despite the constant ankle pain, the safe crossing and a view of snow-frosted trees above elevated my mood. I was going to make it to the spring after all! I would definitely dose myself with pain meds here, and hopefully have less pain on the descent.

What a magical place! There’s a small ledge below the spring where someone had apparently built a cabin a hundred or more years ago – hauling tools and supplies on muleback, cutting native timber. Now all that’s left is the spring and the ledge. I’ve drunk from this spring many times – delicious – but there’s no trail and the slope is too steep to climb in snow. So I just dosed and started back down, trying to keep as much weight off my ankle as possible with the trekking poles.

On the way up, the pain in my ankle had distracted me from discomfort in my left foot, where I have chronic inflammation that was triggered a few weeks ago. I clearly hadn’t recovered, because on the way down I found myself shifting weight to the outside of that foot. And with weight shifted to the outside of both feet, I soon had sharp pain in the outside of both knees. Of course my right shoulder was in constant pain from the long-standing rotator cuff tear, so the 4-1/2 mile descent was an increasing ordeal.

I reached the bottom of the switchbacks, where it was getting very dark. And halfway from there to the trail junction, I suddenly developed cramps in the inside of both thighs. I literally screamed and fell over on the ground, jerking around in excruciating pain, and couldn’t find a position that relieved the cramps. That nightmare went on for about ten minutes.

After the cramps faded away, the ankle and knee pain became bearable! I made it up the final climb out of the canyon just as the sun was setting behind the range in the west. Sitting in the vehicle, I actually felt free of pain for the first time all day. It had taken me 8 hours to go 9 miles out-and-back.

But at home, the minute I tried carrying my gear up the stairs to my back porch, all that knee and ankle pain came back, worse than ever. Even my shoulder was screaming. So I took another dose of meds, and spent the night waking over and over, never able to find a comfortable position. When will I ever learn?

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Letters to My Mother, Part 5: What Are We to Do?

Thursday, January 29th, 2026: Letters to My Mother, Problems & Solutions, Society, Stories, Trouble.

Previous: I Tried to Help


Beliefs, Plans, and Denial

Healthcare Realities

Home Care Realities

Care Home Realities

Life and Death in Long-Term Care

Closing the Cycle

Human Nature

What Are We to Do?


Beliefs, Plans, and Denial

Our Family

Papaw, my dad’s father
Died quickly, in hospital
Of heart failure

Mamaw, his wife, widowed and living alone
Began hallucinating

Her son flew back and tricked her into a nursing home
Said they were going to the doctor
Aides grabbed her from the car
She died miserable, among strangers

My grandpa, your daddy
Died suddenly at home
Of a massive heart attack

Your mother, my grandma
Voluntarily entered a nursing home
Thrived there, singing, comforting
Cheering the other residents

My dad, your first husband
Found freelance home helpers by word of mouth
Paid them minimum wage
Lived at home, managing his own affairs
Until he died during a final trip to the ER

You never made plans for the end of your life
Refused to talk about it
Said you would never leave your home
Would rely on home help when the time came

I believed you irresponsible, living in denial
Until I realized that in the culture of our ancestors
Traditions in family and community
Provided for the end of life
Individuals were not forced to figure it out for themselves

My Friends

In our society, you were at one end of the spectrum
Some of my friends are at the other
Always worried about the future
They devote time and energy to planning for their end

One friend worries about dementia
Worked to create legal provisions for assisted suicide
If he begins to lose his mind

But as we found
Mental illness can defy science

Losing your mind
You could still think and remember
You were afraid to die
And you fought for your life, even while unconscious

What would the law say about that?
Is it really possible to plan for losing your mind?

Other friends prepare for the end of life
By buying long-term care insurance
Implicitly planning to spend their final days in facilities
Like the ones that failed us

Some voluntarily move into “retirement communities”
When they get tired of maintaining their homes
Long before they actually need home care
They like the idea of having care
Available onsite when they need it

With visions of daily golf or bridge
They don’t mind being sequestered among other old people
Isolated from community, families, and youth

Having spent two years
Seeking and working with the kind of care
Many people expect to be available
I believe we’re all in denial

With healthcare and elder care commodities
In our statist, capitalist, bureaucratic society
The kind of care many expect simply doesn’t exist

And often, we are forced into situations
We never could have planned for
Hospitalized with a sudden, unexpected crisis
Suddenly ending up in permanent long-term care

My End

As someone whose quality of life
Depends on hiking and making music, art, and stories
I want my life to end
When I can no longer do those things

I want my life to end
Before I become dependent on the care of others

The rural Irish lived in homes
That included apartments for their elders
When the elders were too old to tend the farm
They moved out of the main house
And became advisors to the young

Traditional societies around the world
Facing limited resources
Condoned suicide by elders
Who could no longer care for themselves

Stories of grandparents jumping or thrown off cliffs
Abandoned on ice floes
Trudging off alone in winter

In our colonial culture
Suicide is such a deep and strong taboo
Science is discouraged from studying these practices
And with our deep puritanical bias
We outlaw voluntary drug overdoses

When friends ask
I tell them when the time comes
I’ll just walk out into the wilderness
But what if it’s too late
And I can no longer get there on my own?

Healthcare Realities

Doctors and Hospitals

Your primary care doctor retired
Just before your final crisis began
Her office made no attempt
To find you a replacement

Our loved ones’ decline often begins in a crisis
Where they end up in the ER
The emergency department of a hospital

The goal of the ER is to rush a diagnosis,
Treatment, and discharge
Frequently, they’re wrong

A loved one must be onsite
To ensure you’re adequately examined
Safely discharged to a place with adequate care
Receiving timely follow-up with a physician

If a patient is in danger of dying
Staff will ask
Do you want us to save you?

This is called Full Code
Involving CPR, intubation, defibrillation
Breaking ribs, puncturing lungs
Risking severe disabilities

If the patient is hard of hearing or confused
By strangers and an unfamiliar environment
They will typically agree

This decision is impossible for family to change
Doctors agree it’s wrong, but that’s the system

If the patient is unable to make a decision
The nurse on hand calls and wakes up next of kin
In the middle of the night, demanding an immediate decision

When your condition is critical
But you need more than a few hours
Of testing and treatment
They admit you to Med Surg

It’s a catch-all unit
Where your case is supervised by a hospitalist
Coordinating a team of specialists

But not all hospitals have all the relevant specialties
And in our colonial society’s reductive paradigm
Specialists have no interest in
Or knowledge of other specialties

They regularly claim authority
And make false conclusions, even let patients die
Based on ignorance
And a narrow perspective

If the issue is behavioral or mental
A hospital psychiatric unit should be the last resort
These units are designed like prisons
To restrain and prevent violent behavior

Because you had no PCP during your crisis
When you were discharged from hospital
There was no follow-up
No confirmation that diagnosis was correct
No confirmation that treatment was successful

Money and Care

Some people will assume that our problems
Resulted from limited and substandard healthcare
In our hometowns
The capital of a notorious red state, and a remote rural town

Many people assume the best healthcare can be found
In affluent enclaves in New York, Boston, the Bay Area, Los Angeles
Minneapolis or Phoenix, with their Mayo Clinics

But the real picture is much more complicated
Yes, I had to fly to Seattle for specialized hip surgery
And to San Francisco for nonsurgical foot treatment
I could afford that, even in my low-income bracket
So there was no need to live in those places

Critical patients in small towns are always referred to cities
For specialist treatment not available locally
But you had an excellent heart surgeon in your Midwestern city
And our small-town psychiatrist was likewise exceptional

Home Care Realities

With few exceptions, our homes and our parents’ homes
Are not designed to be accessible
And most could not be adapted for parents with mobility issues
Parents who need outside caregivers
Requiring their own space and facilities in the home

Our ancestors cared for their parents at home
The architecture and skills handed down by tradition
I yearned to restore that tradition
But dreaded the need when I saw it coming

Our society fails to train us to be caregivers
Like everything else, caregiving is commodified
With low pay, high burnout and turnover

Home care agencies abound in every community
But unless you can prove low income and assets
Qualifying for Medicaid
Private pay is your only option
$30-40 per hour

My dad found freelance home help by word of mouth
Most of them were adequate
For you and your disabled son, I hired an agency
Most caregivers, supposedly trained
Were hopeless and had to be replaced

Nearing the end, when you needed 24/7 monitoring
An agency promised that home care was an option
We agreed on 8 hours per day
With me taking care of you during the remaining 16 hours

But at the last minute
Discovered caregivers are unavailable overnight
On weekends or holidays
So when could I sleep, or take a break?
Forget about overnight trips or vacations

Care Home Realities

Types and Differences

Depending on our degree of independence and need for care
Our colonial, statist, capitalist, bureaucratic society
Offers a spectrum of facilities
As service commodities we can purchase or qualify for
Depending on our financial status

These facilities are most often designed
To offer a continuum of care
In which we can progress from more independence
To more care, as we decline
And most are owned or franchised
By national or regional corporations

Those who actually prefer to age among their peers
Sequestered from the rest of society
Can move to a facility with private homes, duplexes
Or apartments where “seniors” can live
As independently as they please

These are called retirement communities,
Senior living, independent living, etc.

Both my parents experienced health crises
After which they were discharged to a short-term rehab facility
Intended to prepare them to return home

Rehab is basically a skilled nursing facility
A short-term nursing home, part of the continuum of care
So that when a patient fails rehab, they can move directly
Into long-term care

And short-term rehab is covered by Medicare

Assisted living refers to an apartment complex
Where residents can live independently
With onsite access to as much care as they may need

Assisted living facilities may stand alone
Or may be part of a continuum of care
For qualified low-income residents,
Room and board are covered by Medicaid

In the facilities I reviewed
Private pay can range from $3,000 to $9,000 per month
Large corporate facilities at the low end
Small privately-owned facilities at the high end

Memory care refers to long-term residential care
Primarily for those diagnosed with dementia
But as your case showed, they may accept
Anyone struggling with behavioral issues

These are secure units
Typically requiring a keypad code for entry

They may be designed more as homes
Or more as skilled nursing facilities
In any case, memory care facilities may stand alone
Or may be a unit within a larger continuing care facility

Again, Medicaid pays for room and board
And private pay ranges from $10,000 monthly

Those who need help with medications
And activities of daily life (ADLs) in general
Such as dressing, toileting, hygiene, and feeding
Typically end up in long-term care

A skilled nursing facility
Traditionally known as a nursing home
With rooms like in a hospital
Shared or private

For those unqualified for Medicaid
Private pay ranges from $10,000 per month

The larger urban facilities we encountered
Encompassed all types in one building:
Short-term rehab, assisted living apartments,
Memory care and long-term skilled nursing units

Finding a Facility

Image Versus Reality

National magazines with retired subscribers
Have always been full of ads
For supposedly elite elder care facilities
Mostly in the East

My Stanford alumni magazine has glossy full-page ads
For “senior living communities” in affluent enclaves
Like Carmel Valley

But the places with big advertising budgets
Are the places that are not good enough
To survive on word-of-mouth
That’s the way advertising works

And even if we got our parents into one of those places
We wouldn’t be able to visit them regularly

Some believe that more money
Will get you better care
That’s how we’re indoctrinated
In a capitalist economy

But that’s not what I found
The best places I found are the smallest and hardest to get into
They may or may not be the most expensive

But because they’re small
The elite homes
Soon become confining, claustrophic

I suspect the really rich
Are able to offer incentives and accommodations
For paid, live-in caregivers at home

I’ve driven past, and been referred to
Huge facilities with hundreds of apartments or rooms
Landscaped grounds, vegetable gardens
Bistros, pools, theaters
I would never place a loved one there

The best places I found in Indianapolis and Tucson
Were private homes staffed by the owners
And small, locally-owned facilities
Designed around family-centric models
But all those had waiting lists

And because you weren’t able to plan ahead
Our needs were urgent
We had to settle for places with immediate openings

Our Experience

In your metro area of Indianapolis
With a population of nearly a million
An online search returns about 20 elder care homes

The search for Carmel, the affluent northern suburb
Returns an additional 15
There will be lower numbers for suburbs
To east, west, and south

Hence, for a big city
Dozens of options within weekly driving distance
But due to uneven property values
Typically located far from our homes and workplaces

Most of these follow the “continuing care” model
With units for rehab, assisted living, memory care
And long-term skilled nursing

Like most – maybe all large cities
Indianapolis has placement agents for elder care
An agency I worked with has “scouts” for each part of the city
But they only provide placement at large corporate chains

Tucson, with the same population as Indianapolis
Has an agent that will identify and show you
Options to meet your specific needs
At a broad range of facilities
From corporate chains to private homes

Overwhelmed by choices
And the unreliability of online ratings
I followed personal recommendations
From people I trusted
But was disappointed anyway

Life and Death in Long-Term Care

Management

All the management I dealt with
At every facility
Showed two faces
Friendly and caring at first

Then, if family takes a close interest in their loved one’s care
Management reacts to suggestions defensively
Reacts to issues offensively
Blames resident or family
Before considering their own responsibility

They all exhibited a top-down culture
In which management behavior
Was imitated by staff

Dishonesty, manipulation, and retaliation were common
Management always spoke with authority
Of residents’ conditions and mood
When they never spent time alone with residents
Never engaged residents in substantive conversations

They get away with all this
Because it’s a seller’s market
They have waiting lists
Can reject you and move on

Family Relations

Again and again, I’ve heard from friends
About what a wonderful home they found
For their parent

And over and over, in care facilities
I’ve met residents who are lonely and bitter
Because their loved ones abandoned them there
And seldom if ever visit

I did meet a few – less than ten percent
Who say they’re content

In my grandparents’ generation
If elders went into a care facility
Their children and grandchildren
Lived only a few blocks away
Visited after work or school

In our highly mobile society
Where families are dispersed across continents
Sometimes across oceans
Children are used to going months
Without seeing their parents

Most care facilities are designed to replace the family
Encourage residents to trust staff
Attempt to foster community among residents
Why do families accept that?

Because most families have no room for elders
They have careers, children of their own
Or want to enjoy their retirement
Visit their loved ones only at their convenience

In our blind worship of progress
We’ve abandoned native traditions
Elders no longer accumulate stories and wisdom
That could help us and keep them engaged

Different facilities have different policies
Some allow visits 24/7
Some provide meals for visitors
A few may even have overnight accommodations

Many facilities, designed for staff convenience
Create barriers against both visits and outings
Long walks from parking
Long interior hallways
A series of locked doors or gates
Some requiring staff to open

Others, like your final home
Only allow visits during limited hours
Don’t allow family to share meals

Conditions

Facilities are typically designed and managed
For staff convenience first
Resident comfort second

At the time in your life
When you’re least resilient, least adaptable
These facilities force you into a schedule
For their own convenience
Confusing you, making you feel helpless

The hearts of these facilities are the nurse’s stations
And the dining rooms

Once you’re identified as a fall risk
Fearing liability, institutions will confine you to bed
Limit your mobility to a wheelchair
May even confine you to the nurse’s station
Sleeping all day, slumped in your wheelchair

The hearing impaired
Can’t communicate adequately with staff
So their health conditions
Are never fully known or treated
And they’re frustrated in group activities and events

Many facilities advertise chef-cooked meals
Made from healthy, fresh, even local ingredients
But even at the highest-rated facilities
This is often merely marketing hype

The only way to tell is to visit at mealtime
Day in and day out
Who can do that?

Even the best facilities lack the ability
To offer personalized food
On a personalized schedule

Dysphagia (difficulty swallowing)
And aspiration (accidentally inhaling while drinking or eating)
Are common among elders

We can easily train ourselves
To eat and drink safely
But with the liability of choking
Institutions force residents onto a pureed diet
Where, unable to recognize their food
They lose weight and weaken

You literally starved to death
Because your home could not give you
What you liked, when you needed it

Many homes have no way
For residents to call for help

Even with call buttons
With 8-12 residents per aide
It can take up to 45 minutes
For a resident to get help
Lying in a soiled bed

If you yell, staff get angry
Or make fun of you

Good staff are hard to find
With high burnout and turnover

Some are good at what they do, and care
Many of them are studying, for higher pay
And will move on soon
Most are just burnt out, collecting a paycheck

What they call activities and entertainment
Are designed for the lowest common denominator
Bingo, juvenile cliches, celebrities
Insecure, embarrassing volunteers

I always found wonderful people
Both staff and volunteers
Who deserve endless praise for showing up
Giving their heart, soul, and time
But they were in the minority

Hospice

When you are admitted to hospice
You fall under the care of a doctor you will never see
Their primary function to prescribe medications
At the request of a nurse
Who visits you weekly

Under Medicare rules
You’re ineligible for most therapies, treatments
Or visits to doctors
You can still get them on a private pay basis

For us, the result was that I became your doctor
I saw you the most, spent the most time with you
Since I was the only one you trusted
I had the most accurate experience of your symptoms

I studied and requested your medications
If I hadn’t been available
Symptoms would’ve been missed
Your care would’ve suffered

Our big-city hospice provider was wonderful
Professional help available 24/7
On call nurse within 30 minutes
Social worker helped find resources, completed paperwork

Small-town hospice had limited staff
Completely lacking some functions
No help in a crisis
Their social worker a disaster

We loved your hospice nurses
And some of your hospice aides
Who came to bathe you two or three times a week
Provide personal care as needed

Hospice promises to provide comfort at the end of life
I discovered that was a lie
Not even morphine could relieve your suffering
In the final days

Closing the Cycle

The colonial tradition brought by our English founders
And still observed in conservative families
Is to preserve the body by chemical embalming
Hold an open casket funeral for viewing by the community
Followed by underground burial officiated by a pastor
With the goal of protecting the physical body
From returning to its natural elements

Indigenous societies worldwide
Implemented a variety of practices
Ranging from burial to abandonment and cremation

Our bodies came from the earth
Evolving and rebuilding constantly
From the resources we ingest
Ultimately originating in nature
Clouds, rocks, rivers, soils, plants, animals

Burial and cremation, while practical in some habitats
Deny nature the resources she gifted us
This is recognized today in colonial society
By a tiny minority in the natural burial movement

You asked for cremation
I planned to honor your wishes
But when the time came I was unprepared
Had no idea what would happen

I had to choose a funeral home
The funeral director came, I had to leave
They took your body away
Put you in cold storage, as found

I had to get permission from the state
To have you cremated
I waited all week
Wanting to be with you

I vaguely knew that in our ancestral tradition
Family and others from the church
Washed, dressed, and casketed the body for burial
I had no idea what would happen to your body
Wanted to be a part of that
But had never been trained

It turned out that you would just be conveyed from storage
Into the chamber, for incineration
By strangers
Burning and cooling would take hours

I thought of waiting outside
But it’s a big building
There would be nothing to see

In the end, I received your ashes
In a plastic bag
Inside a plastic box

Human Nature

An institution is only as good as its people
What happens to the people
When society itself is dysfunctional
And its institutions are failing?

The villains of your story
The corrupt police and prosecutor
Your troubled second husband and his insecure daughter
The arrogant, ignorant doctors and facility managers
The cruel and thoughtless aides

They all hurt us
In some cases terribly
In some cases repeatedly, over time

But we understood them, you and I
None of them is all bad

Like you said, most of them were two-faced
Sometimes kind, sometimes cruel
Insecure, damaged people
Taking out their own fears on the weak, the helpless

Their jobs some of the most difficult
Shouldn’t be jobs in the first place
Should be traditional roles in a healthy community
Not careers in an economy

What Are We to Do?

Our statist, capitalist model
For elder care as a commodity
The result of what we believe
To be generations of “progress”
Works no better than our other institutions

The only healthy way to care for elders
Is within healthy families
Within healthy communities

Which our society fails to create or cultivate
Which our “progress” actively destroys
Via technologies of mobility and long-distance communication

What we are left with is institutional care
Subsidized by the state at generally low standards
Or purchased by us at from $36,000 to $144,000 per year
Depending on the level of care we need

A decade ago
I fought your husband’s estate
For a settlement that would keep you secure
But there was no way I could predict
Your ultimate needs

During your last year
When you were nearing the highest level of care
Not knowing how long you would last
I worried about running out of money

I assumed that if you had a prognosis of a few weeks
And if I could find home help
We could afford to keep you at home

But in the end, home help was only available
During regular business hours
Leaving me on duty overnight and all weekend

I assumed that if you had a prognosis of a few years
We could afford to keep you in a care facility
But science can’t provide a prognosis that accurate

I believe that as families
The closest we can come
To a healthy traditional model for aging and dying
Is to provide lodgings for our elders in our homes

And when they need care, to enlist family
And community, providing care in the home

But since technology disperses our families
And capitalism leaves us burnt out
And isolated, on a fixed income
When our elders need care
This model is only available
To the very wealthy

Based on our experience
The second best model is emerging
In large metro areas
Families who convert their homes
Into private elder care facilities

With typically 4 to 6 bedrooms
These facilities are in great demand
And typically have long waiting lists
Sometimes years

Hence they’re not options we can rely on
Because who can plan
When their elders will need help?

For those of you who worry about the future
What’s your plan for civil war?
What’s your plan for economic collapse?

Science could not explain or treat your suffering
Drugs could not relieve it
Care homes could not provide loving care
Hospice could not comfort you at the end
Society does not allow our bodies to return to nature

What are we do to?

 


 

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